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网站主页 甲醇中4种药物混标/BJS 201701 标准品/甲醇中4种药物混标/BJS 201701
  • 标准品/甲醇中4种药物混标/BJS 201701

标准品/甲醇中4种药物混标/BJS 201701

￥20 1 起订
更新日期：2026-01-29

坛墨质检科技股份有限公司

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产品详情:

中文名称：
标准品/甲醇中4种药物混标/BJS 201701
品牌：
TMstandard
货期：
现货
库存：
≥6
编号：
81810a
过期日期：
2025-01-04
标准值100μg/mL

甲醇中4种药物混标

CAS号 名称 标准值 单位
58-94-6 氯噻嗪 100 μg/mL
58-93-5 氢氯噻嗪 100 μg/mL
81131-70-6 普伐他汀钠 100 μg/mL
54-31-9 呋塞米 100 μg/mL

Reference Material

This certificate is designed in accordance with ISO 17034 and ISO Guide 31. This reference material (RM) was designed,produced and verified in accordance with ISO/IEC 17025, ISO 17034 and a registered quality management system ISO 9001.

Product Name(产品名称) 4 Drug Mix in Methanol,100μg/mL(甲醇中4种药物混标)
Part Number(产品编号) 81810a
Lot Number(产品批号) -
Expiry Date(失效日期) 2026-Apr-02________________________
Storage(存储条件)           (2-8)℃
                                                        冷藏(2~8)℃
Transportation(运输条件)         Normal temperature transportation
                                                              (常温运输)
CERTIFIED
Component
No.
(组分数) 		Peak
Sequence
(出峰顺序) 		Component
(组分) 		CAS No. Concentration
(μg/mL)
(浓度) 		Relative Expanded
Uncertainty(%) (k=2)
(相对扩展不确定度)
1 1 Chlorothiazide (氯噻嗪) 58-94-6 100 3
2 2 Hydrochlorothiazide (氢氯噻嗪) 58-93-5 100 3
3 3 Pravastatin Sodium1 (普伐他汀钠) 81131-70-6 100 3
4 4 Furosemide (呋塞米) 54-31-9 100 3
Instrument(检测仪器)   HPLC/DAD
Column(色谱柱)   C18(3.0x100mm,1.8μm)
Column Oven(柱温)   35℃
Wavelength(波长)   230nm
Method Details(方法参数)
  A：0.1% Phosphoric Acid(0.1% 磷酸)
  B：Acetonitrile(乙腈)
Time/min A/% B/%
0.00 90 10
0.50 90 10
4.00 10 90
8.00 10 90
8.10 90 10
Note

1.The standard value of pravastatin sodium is  pravastatin.(普伐他汀钠的标准值以普伐他汀计)

Intended Use

This RM is intended for use in a laboratory as a calibration and quality control standard or in method development for analytical techniques.

Uncertainty

The certified value(s) and uncertainty(ies) are determined in accordance with ISO 17034 with an 95% confidence level (k=2). Uncertainty is based on the Total Combined Uncertainty, including uncertainties of preparation, purity of neat materials, homogeneity, stability testing.

Traceability

The balances used for gravimetric measurements are calibrated with weights traceable to the national standards. The calibration of the balances is verified annually by an external accredited calibration service. This analysis method has been verified using an approach consistent with ISO 17034:2016 & ISO 17025:2017.

Homogeneity

Random replicate samples of the final packaged RM have been analysed to prove homogeneity consistent with ISO 17034.

Storage

The RM should be stored in the original sealed bottle at the indicated temperature.

CERTIFICATE    ON QC    SIGNATURE
- RM Release

相关产品信息
编号产品名CAS规格品牌价格过期时间
81810a标准品/甲醇中4种药物混标/BJS 2017011mLTMstandard4002026-04-02
81810a标准品/甲醇中4种药物混标/BJS 2017011mLTMstandard202025-01-04
标准品/甲醇中4种药物混标/BJS 201701;标准品/甲醇中4种药物混标/BJS 201701价格;标准品/甲醇中4种药物混标/BJS 201701厂家;TMstandard

公司简介


成立日期 (8年)
注册资本 5000万人民币
员工人数 100-500人
年营业额 ￥ 500万-1000万
经营模式
主营行业

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